Canonical Allele Identifier: CA2665620101

Gene: COL7A1

Linked Data

• gnomAD v4: 3-48568768-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568768C>T , CM000665.2:g.48568768C>T	GRCh38
NC_000003.11:g.48606201C>T , CM000665.1:g.48606201C>T	GRCh37
NC_000003.10:g.48581205C>T	NCBI36
NG_007065.1:g.31485G>A , LRG_286:g.31485G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7758+16G>A MANE Select	ENSP00000506558.1:n.7758+16G>A
ENST00000328333.12:c.7758+16G>A	ENSP00000332371.8:n.7758+16G>A
ENST00000459756.5:n.581+16G>A
ENST00000467985.1:n.604+16G>A
ENST00000487017.5:n.4397+16G>A
NM_000094.3:c.7758+16G>A , LRG_286t1:c.7758+16G>A	NP_000085.1:n.7758+16G>A
XM_011533336.1:c.7785+16G>A	XP_011531638.1:n.7785+16G>A
XM_011533337.1:c.7758+16G>A	XP_011531639.1:n.7758+16G>A
XM_011533338.1:c.7725+16G>A	XP_011531640.1:n.7725+16G>A
XM_011533339.1:c.7785+16G>A	XP_011531641.1:n.7785+16G>A
XR_940369.1:n.7821+16G>A
XR_940370.1:n.7821+16G>A
XR_940371.1:n.7821+16G>A
XR_940372.1:n.7795+16G>A
XM_017005688.1:c.7698+16G>A	XP_016861177.1:n.7698+16G>A
XM_017005689.1:c.7758+16G>A	XP_016861178.1:n.7758+16G>A
XR_001740003.1:n.7794+16G>A
XR_001740004.1:n.7794+16G>A
XR_001740005.1:n.7794+16G>A
XR_001740006.1:n.7768+16G>A
NM_000094.4:c.7758+16G>A MANE Select	NP_000085.1:n.7758+16G>A